576166
1-(2-Hydroxyethyl)imidazole
97%
동의어(들):
1-(β-Hydroxyethyl)imidazole, 1-(2-Hydroxyethyl)-1H-imidazole, 1-(2′-Hydroxyethyl)imidazole, 2-(1H-Imidazol-1-yl)ethan-1-ol, 2-(1H-Imidazol-1-yl)ethanol, 2-(1′-Imidazolyl)ethanol, 2-(Imidazol-1-yl)ethanol, N-(2-Hydroxyethyl)-1H-imidazole, N-(2-Hydroxyethyl)imidazole
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모든 사진(1)
About This Item
추천 제품
Quality Level
분석
97%
형태
solid
mp
36-40 °C (lit.)
SMILES string
OCCn1ccnc1
InChI
1S/C5H8N2O/c8-4-3-7-2-1-6-5-7/h1-2,5,8H,3-4H2
InChI key
AMSDWLOANMAILF-UHFFFAOYSA-N
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
>230.0 °F - closed cup
Flash Point (°C)
> 110 °C - closed cup
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
ACS applied materials & interfaces, 11(3), 2860-2869 (2018-12-27)
Gram-negative bacteria, containing toxic proinflammatory and pyrogenic substances [endotoxin or lipopolysaccharide (LPS)], can lead to infection and associated serious diseases, such as sepsis and septic shock. Development of antimicrobial materials with intrinsically endotoxin adsorption activity can prevent the release of
Analytical and bioanalytical chemistry, 408(30), 8655-8661 (2016-08-06)
The online combination of capillary electrophoresis (CE) with mass spectrometry (MS) has long been desired for the capability of direct and simultaneous separation and detection with high efficiency, accuracy, and throughput. In this work, a novel CE-MS interface was developed
Journal of chromatography. A, 1620, 461013-461013 (2020-03-24)
Dummy molecularly imprinted microspheres (DMIMs) were synthesized by Pickering emulsion polymerization and used as the matrix solid-phase dispersion extraction (MSPD) sorbent for sample pre-treatment of azole fungicides in fish samples. Alpha-(2,4-Dichlorophenyl)-1H-imidazole-1-ethanol (DCE) was used as the fragment dummy template for
Nature communications, 11(1), 6242-6242 (2020-12-09)
DNA-templated synthesis takes advantage of the programmability of DNA-DNA interactions to accelerate chemical reactions under diluted conditions upon sequence-specific hybridization. While this strategy has proven advantageous for a variety of applications, including sensing and drug discovery, it has been so
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